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A. Mohamed · SciRah

Researcher profile · Semantic Scholar

A. Mohamed

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A. Mohamed — researcher profile on SciRah

h-index: 8
Works: 41
Citations: 200

Most-cited papers

Phenotypic and cytogenetic spectrum of 9p trisomy.
S. Temtamy, A. Kamel, S. Ismail, N. Helmy +4 more
2007Genetic Counseling53 citations
Semantic Scholar
Isodicentric Y chromosomes in Egyptian patients with disorders of sex development (DSD)
M. Mekkawy, A. Kamel, M. El-Ruby, A. Mohamed +5 more
2012American Journal of Medical Genetics. Part A17 citations
Semantic Scholar
Bladder exstrophy and extreme genital anomaly in a patient with pure terminal 1q deletion: expansion of phenotypic spectrum.
Maha S. Zaki, G. Gillessen-kaesbach, I. Vater, A. Caliebe +4 more
2012European Journal of Medical Genetics17 citations
Semantic Scholar
Clinical features of SMARCA2 duplication overlap with Coffin–Siris syndrome
N. Miyake, G. Abdel-Salam, T. Yamagata, Maha M. Eid +11 more
2016American Journal of Medical Genetics. Part A15 citations Open access
Semantic Scholar
Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly
A. Mohamed, A. Kamel, M. Eid, Ola M. Eid +17 more
2021Molecular Genetics & Genomic Medicine13 citations Open access
Semantic Scholar
Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature
M. Mekkawy, A. Kamel, M. Thomas, E. Ashaat +12 more
2020Molecular Genetics & Genomic Medicine12 citations Open access
Semantic Scholar
Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation
A. Mohamed, H. El-Bassyouni, A. El-Gerzawy, S. Hammad +6 more
2018Molecular Cytogenetics9 citations Open access
Semantic Scholar
Emanuel syndrome due to unusual segregation of paternal origin.
Maha S. Zaki, A. Mohamed, A. Kamel, A. El-Gerzawy +1 more
2012Genetic Counseling8 citations
Semantic Scholar
Cyclin D1 gene amplification in proliferating haemangioma
A. Mohamed, Tarek F. Elwakil, Ibrahim M. Taher, M. Elbarbary +3 more
2009Cell and Tissue Research8 citations
Semantic Scholar
Developing a Road Map to Spread Genomic Knowledge in Africa: Meeting Report: 10th Conference of the African Society of Human Genetics, Cairo, Egypt.
Ghada Y El-Kamah, A. Mohamed, Y. Gad, S. Abdelhak +7 more
2019American Journal of Tropical Medicine and Hygiene7 citations Open access
Semantic Scholar
Expansion of the phenotypic and mutational spectrum of Carpenter syndrome.
Rabab Khairat, R. Elhossini, N. Sobreira, Elizabeth Wohler +7 more
2021European Journal of Medical Genetics6 citations Open access
Semantic Scholar
Interstitial Deletion of 2q22.2q22.3 Involving the Entire ZEB2 Gene in a Case of Mowat-Wilson Syndrome
Khaled M Refaat, N. Helmy, M. Elawady, M. El Ruby +6 more
2021Molecular Syndromology4 citations Open access
Semantic Scholar
Contribution of chromosomal abnormalities at 10q and 22q to autism
N. Meguid, M. Eid, A. Mohamed, Heba Ghanoum +2 more
2018Research in Autism Spectrum Disorders4 citations
Semantic Scholar
An infertile azoospermic male with 45,X karyotype and a unique complex (Y;14); (Y;22) translocation: cytogenetic and molecular characterization
M. Mekkawy, Ahmed M. El Guindi, I. Mazen, A. Fayez +2 more
2018Journal of Assisted Reproduction and Genetics4 citations Open access
Semantic Scholar
Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features
M. Zaki, Ola M. Eid, M. Eid, A. Mohamed +3 more
2019Cytogenetic and Genome Research3 citations
Semantic Scholar
Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion
M. Eid, Ola M. Eid, I. Hegazy, Marian Y. Girgis +2 more
2019Neuropediatrics3 citations
Semantic Scholar
Genetic diagnosis of Prader–Willi syndrome
A. Khedr, N. Meguid, A. Mohamed, S. Ismail +3 more
20163 citations
Semantic Scholar
A Unique Derivative Chromosome 4 with a Predominant 4p16.3 Microduplication Phenotype and a Literature Review
M. Mekkawy, A. Kamel, Khaled M. Refaat, Abdelrahman Madian +5 more
2024Molecular Syndromology2 citations Open access
Semantic Scholar
Unbalanced 14;X Translocation and Pattern of X Inactivation in a Female Patient with Multiple Congenital Anomalies
A. Mohamed, M. Zaki, A. Kamel, M. Issa +3 more
2018Cytogenetic and Genome Research2 citations
Semantic Scholar
Clinical and cytogenetic description of three patients with constitutional mosaic trisomy 8
S. Ismail, A. Kamel, M. Eid, M. Elruby +6 more
20172 citations
Semantic Scholar
Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study.
H. El-Bassyouni, A. El-Gerzawy, A. Mohamed, A. Kamel +3 more
2014Genetic Counseling2 citations
Semantic Scholar
Study of Her-2/neu and TOP2A expression in familial versus sporadic breast carcinoma
A. El-Gerzawy, Mervat Al Ansary, Iman L. Hussein, A. Mohamed +3 more
20132 citations Open access
Semantic Scholar
Clinical and molecular cytogenetic description of a female patient with de novo 18q inversion duplication/deletion
Rana Mahrous, M. Gabal, Ola M. Eid, E. Ashaat +3 more
2021Gene Reports1 citations
Semantic Scholar
Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant
H. Afifi, Ghada Y El-Kamah, A. Kamel, Sally G. Abd Allah +4 more
2020Journal of Pediatric Genetics1 citations Open access
Semantic Scholar
Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation
A. Mohamed, M. Eid, Ola M. Eid, Shymaa H. Hussein +6 more
2020Cytogenetic and Genome Research1 citations
Semantic Scholar
Cytogenetic study of a large cohort of patients with corpus callosum abnormalities
D. Hussen, A. Kamel, M. Mekkawy, A. Mohamed +7 more
20191 citations
Semantic Scholar
Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22
E. Ashaat, S. Ismail, A. Kamel, A. Mohamed +5 more
20181 citations
Semantic Scholar
Phelan–McDermid Syndrome: Expanding the Phenotype
H. El-Bassyouni, Ola M. Eid, S. Ismail, M. El-Ruby +9 more
2022Middle East Journal of Medical Genetics0 citations Open access
Semantic Scholar
Breast Screening Using 3D Automated Breast Ultrasound in Addition toConventional B Mode Ultrasound
A. Mohamed, K. Lakouz, Ahmed Abd Al Azim, Mona +1 more
20210 citations
Semantic Scholar
ROLE OF 3D AUTOMATED BREAST ULTRASOUND AS A FUTURE BREAST SCREENING TOOL IN ADDITION TO MAMMOGRAPHY
A. Mohamed, K. Lakouz, Ahmed Abd Al Azim, M. Refaat
20210 citations
Semantic Scholar
Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion
Assad S. Elgerzawy, A. Kamel, M. El Ruby, S. Hammad +5 more
20190 citations
Semantic Scholar
EFFECT OF RESVERATROL ON GENOMIC STABILITY IN FANCONI ANEMIA
P. Fahmy, M. Ragab, A. Mohamed, M. Eid +1 more
20190 citations Open access
Semantic Scholar
Cytogenetics abnormalities in a referred population for chromosomal analysis and the role of fluorescence in-situ hybridization in refining the diagnosis
A. Mohamed, A. Kamel, N. Helmy, S. Hammad +14 more
20170 citations
Semantic Scholar
Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies
M. Mekkawy, I. Mazen, A. Kamel, W. Mahmoud +1 more
20160 citations
Semantic Scholar
Cytogenetic Variability and Phenotypic Findings in Patients with Ovotesticular Disorder of Sex development
M. Mekkawy, I. Mazen, A. Kamel, A. Mohamed +1 more
20160 citations
Semantic Scholar
The association of polymorphism of catechol-O-methyltransferase and karyotype abnormalities in disabled children
Hoda M. Abd El-Ghany, Aisha M. Abd El-Rahman, Sawsen M. Abd El-Hady, A. Mohamed +2 more
20150 citations
Semantic Scholar
Role of Sex Chromosomal Abnormalties in Cases of Primary Amenorrhea
Nagham A. El Ameer, N. A. Megiud, A. Mohamed
20130 citations
Semantic Scholar
Fanconi anemia: studying telomeres and telomerase genes using fluorescent in-situ hybridization technique in Egyptian patients
S. Temtamy, M. Eid, A. Mohamed, Hesham F. Kayed +2 more
20110 citations Open access
Semantic Scholar
Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome
A. Mohamed, A. Kamel, K. Hf, Meguid Nm +1 more
20090 citations
Semantic Scholar
Chromosomal Alterations in Ulcerative Colitis
M. Shehab, Soheir A. Elkawy, A. Mohamed, N. Elwan +4 more
20090 citations
Semantic Scholar
Genomics research in Africa: implications for disease diagnosis, treatment and drug development: proceedings of the 5th annual meeting of the African Society of Human Genetics
M. Newport, Sonia Abdelhaq, Emal Abulezz, A. Adeyemo +8 more
20080 citations
Semantic Scholar

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